Associations between acute glucose control and peripheral nerve structure and function in type 1 diabetes.


Journal

Diabetic medicine : a journal of the British Diabetic Association
ISSN: 1464-5491
Titre abrégé: Diabet Med
Pays: England
ID NLM: 8500858

Informations de publication

Date de publication:
09 2020
Historique:
accepted: 09 04 2020
pubmed: 17 4 2020
medline: 5 10 2021
entrez: 17 4 2020
Statut: ppublish

Résumé

To examine the associations between continuous overlapping net glycaemic action (CONGA), percentage time in hyperglycaemia (%HG) or normoglycaemia (%NG) and peripheral nerve structure and function in type 1 diabetes. Twenty-seven participants with type 1 diabetes underwent continuous glucose monitoring followed by corneal confocal microscopy and nerve excitability assessments. CONGA, %HG (> 10.0 mmol/l) and %NG (3.9-10.0 mmol/l) were correlated against corneal nerve fibre length and density in the central cornea and inferior whorl region, corneal microneuromas, and a nerve excitability score while controlling for age, sex, diabetes duration and HbA An increase in CONGA [median 2.5 (2.0-3.1) mmol/l] or %HG (mean 46 ± 18%) was associated with a worse nerve excitability score (r = -0.433, P = 0.036 and r = -0.670, P = 0.0012, respectively). By contrast, greater %NG (51 ± 17%) correlated with better nerve excitability scores (r = 0.672, P = 0.0011). Logistic regression revealed that increasing %HG increased the likelihood of abnormal nerve function [odds ratio (OR) 1.11, 95% confidence interval (CI) 1.01-1.23; P = 0.037). An increase in CONGA and %HG were associated with worsening nerve conduction measures, whereas longer %NG correlated with improved nerve conduction variables. CONGA and %HG were associated with inferior whorl corneal nerve fibre length (r = 0.483, P = 0.034 and r = 0.591, P = 0.021, respectively) and number of microneuromas (r = 0.433, P = 0.047 and r = 0.516, P = 0.020, respectively). Short-term measures of glucose control are associated with impaired nerve function and alterations in corneal nerve morphology.

Identifiants

pubmed: 32298478
doi: 10.1111/dme.14306
doi:

Substances chimiques

Blood Glucose 0
Hypoglycemic Agents 0
Insulin 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1553-1560

Subventions

Organisme : National Health and Medical Research Council
ID : 1091006
Pays : International

Informations de copyright

© 2020 Diabetes UK.

Références

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Auteurs

T Issar (T)

Prince of Wales Clinical School, Sydney, NSW, Australia.

S S Tummanapalli (SS)

School of Optometry & Vision Science, University of New South Wales, Sydney, NSW, Australia.

N C G Kwai (NCG)

Prince of Wales Clinical School, Sydney, NSW, Australia.
Department of Exercise Physiology, UNSW-Sydney, Sydney, NSW, Australia.

J C B Chiang (JCB)

School of Optometry & Vision Science, University of New South Wales, Sydney, NSW, Australia.

R Arnold (R)

Department of Exercise Physiology, UNSW-Sydney, Sydney, NSW, Australia.

A M Poynten (AM)

Department of Endocrinology, Prince of Wales Hospital, Sydney, NSW, Australia.

M Markoulli (M)

School of Optometry & Vision Science, University of New South Wales, Sydney, NSW, Australia.

A V Krishnan (AV)

Prince of Wales Clinical School, Sydney, NSW, Australia.

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Classifications MeSH